TwoFer Needle 19003

GUDID 00085412478418

TwoFer Huber-Tipped Needle

MEDSAFETY SOLUTIONS LLC

Medication transfer needle, non-filtering/non-vented
Primary Device ID00085412478418
NIH Device Record Key7d7a67d7-65a5-485d-af8b-101e8eac5847
Commercial Distribution StatusIn Commercial Distribution
Brand NameTwoFer Needle
Version Model Number19003
Catalog Number19003
Company DUNS080521478
Company NameMEDSAFETY SOLUTIONS LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-720-500-2500
Emailinfo@medsafetysolutions.com

Device Dimensions

Needle Gauge16 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100085412478418 [Previous]
GS100853832007064 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LHISet, I.V. Fluid Transfer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-08-09
Device Publish Date2017-12-01

On-Brand Devices [TwoFer Needle]

00085412478395TwoFer Huber-Tipped Needle
00085412478418TwoFer Huber-Tipped Needle

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.